Canonical Allele Identifier: CA1226667734
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663368686

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705865del , CM000663.2:g.230705865del GRCh38
NC_000001.10:g.230841611del , CM000663.1:g.230841611del GRCh37
NC_000001.9:g.228908234del NCBI36
NG_008836.1:g.13729del
NG_008836.2:g.13729del

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1097+71del MANE Select ENSP00000355627.5:n.1097+71del
ENST00000679684.1:c.1097+71del ENSP00000505981.1:n.1097+71del
ENST00000679738.1:c.1097+71del ENSP00000505063.1:n.1097+71del
ENST00000679802.1:c.*556+71del ENSP00000505184.1:n.*556+71del
ENST00000679854.1:n.5402+71del
ENST00000679957.1:c.1097+71del ENSP00000506646.1:n.1097+71del
ENST00000680041.1:c.1097+71del ENSP00000504866.1:n.1097+71del
ENST00000680783.1:c.829+4133del ENSP00000506329.1:n.829+4133del
ENST00000681269.1:c.1097+71del ENSP00000505985.1:n.1097+71del
ENST00000681347.1:n.1679del
ENST00000681514.1:c.1097+71del ENSP00000505963.1:n.1097+71del
ENST00000681772.1:c.*67del ENSP00000505829.1:n.*67del
ENST00000366667.4:c.1124+71del ENSP00000355627.4:n.1124+71del
NM_000029.3:c.1124+71del NP_000020.1:n.1124+71del
NM_000029.4:c.1124+71del NP_000020.1:n.1124+71del
NM_001382817.3:c.1097+71del NP_001369746.2:n.1097+71del
NM_001384479.1:c.1097+71del MANE Select NP_001371408.1:n.1097+71del